Abstract
Abstract Acid-catalyzed fluorous benzylating reagents have been developed based on the unique π-electron deficient properties of triazinedione. Alcohols and carboxylic acids could be converted into the corresponding fluorous-benzyl ether and ester derivatives, respectively, in good yield by using the reagents in the presence of a catalytic amount of trifluoromethanesulfonic acid.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
